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Details
Link-It Detail - Disease - Polycythemia Vera
Debug Stats
  • ### Total Build Time: 475 ms 64.009 KB
  • CONCEPT_NAME gt=12 ms Completed: 12 ms rowSize= 332 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 205 bytes
  • Skipping details on: CONCEPT_SYNONYM gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • Skipping details on: CONCEPT_TEXT gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_SEMANTIC_TYPE gt=0 Completed: 0 ms rowSize= 187 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=12 ms Completed: 12 ms rowSize= 564 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=9 ms Completed: 9 ms rowSize= 1.523 KB
  • CONCEPT_RELATIONSHIPS gt=364 ms Completed: 364 ms rowSize= 17.691 KB
  • CONCEPT_GENES gt=65 ms Completed: 65 ms rowSize= 42.350 KB
  • CONCEPT_XREFS gt=12 ms Completed: 12 ms rowSize= 1.151 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Polycythemia Vera C0032463
Definition (1)
a condition that produces excessive red blood cells
Semantic Types (1)
Neoplastic Process (T191)
Parents (1)
img Myeloproliferative Disorders C0027022
Ancestral Roots
RootRoot Plus OneDepthParent
img Hemic and Lymphatic Diseases C0018981img Hematologic Diseases C00189395img Myeloproliferative Disorders C0027022
Relationships (134)

Relation Types:
diso_​to_​anat : 15
diso_​to_​chem : 49
diso_​to_​diso : 61
diso_​to_​gene : 3
diso_​to_​phen : 2
diso_​to_​phys : 4


Relationships:
none : 42
classifies : 1
gene_​associated_​with_​disease : 2
gene_​product_​malfunction_​associated_​with_​disease : 2
inheritance_​type_​of : 2
is_​abnormal_​cell_​of_​disease : 4
is_​normal_​cell_​origin_​of_​disease : 3
is_​normal_​tissue_​origin_​of_​disease : 2
is_​not_​cytogenetic_​abnormality_​of_​disease : 2
is_​not_​finding_​of_​disease : 1
is_​not_​molecular_​abnormality_​of_​disease : 1
is_​not_​normal_​cell_​origin_​of_​disease : 1
is_​primary_​anatomic_​site_​of_​disease : 2
isa : 3
manifestation_​of : 26
mapped_​to : 1
may_​be_​cytogenetic_​abnormality_​of_​disease : 5
may_​be_​finding_​of_​disease : 2
may_​be_​molecular_​abnormality_​of_​disease : 1
may_​treat : 30
permuted_​term_​of : 1
Page Size
Current 25
  Page 1 of 6
Prior Page
Current 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_PHEN233img genetic aspects C0017399
DISO_to_CHEM160img Janus Kinase 2 C0169661
DISO_to_CHEM160img Janus kinase 2 C0169661
DISO_to_DISO140img Complication Aspects C1171258
DISO_to_DISO134img Complication Aspects C1171258
DISO_to_DISO119img Thrombocythemia, Essential C0040028
DISO_to_PHEN89img genetic aspects C0017399
DISO_to_ANAT75img In Blood C0005768
DISO_to_ANAT73img In Blood C0005768
DISO_to_DISO72img Primary Myelofibrosis C0001815
DISO_to_DISO66img ESSENTIAL THROMBOCYTHEMIA C0040028
DISO_to_PHYS59img Mutation C0026882
DISO_to_CHEM30img Cellular Proto Oncogene Proteins C0033712
DISO_to_CHEM30img Protein Tyrosine Kinase C0033681
DISO_to_CHEM30img Protein-Tyrosine Kinases C0033681
DISO_to_CHEM30img Proto-Oncogene Proteins C0033712
DISO_to_DISO30img Thrombosis C0040053
DISO_to_PHYS28img Mutation, Missense C0599155
DISO_to_DISO25img Primary Myelofibrosis C0001815
DISO_to_DISO25img Thrombosis C0040053
DISO_to_CHEM22img Hydroxyurea C0020402
DISO_to_DISO22img Thrombocytosis C0836924
DISO_to_CHEM17img Hydroxyurea C0020402
DISO_to_PHYS17img Mutation, Point C0162735
DISO_to_PHYS15img Mutation, Point C0162735
Genes (53)

Species:
human : 53
Page Size
Current 25
  Page 1 of 3
Prior Page
Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanPPBPL1728045
img NCI, Score=801, Pubmed Id: 93844, UMLKSK CUI: C0032463
img NCI, Score=801, Pubmed Id: 93844, UMLKSK CUI: C0032463
img NCI, Score=801, Pubmed Id: 6194555, UMLKSK CUI: C0032463
img NCI, Score=801, Pubmed Id: 1836999, UMLKSK CUI: C0032463
HumanERVK7449619
img NCI, Score=801, Pubmed Id: 7683217, UMLKSK CUI: C0032463
HumanPSORS1C2170680psoriasis susceptibility 1 candidate 2
img GENERIF, Score=1000, Pubmed Id: 12823445, UMLKSK CUI: C0032463
HumanERVK664006
img NCI, Score=801, Pubmed Id: 7683217, UMLKSK CUI: C0032463
HumanCD17757126CD177 molecule
Click here to display 32 evidence detail records.
HumanPTPN2226191protein tyrosine phosphatase, non-receptor type 22 (lymphoid)
img GENERIF, Score=1000, Pubmed Id: 17854359, UMLKSK CUI: C0032463
HumanL3MBTL126013l(3)mbt-like 1 (Drosophila)
img NCI, Score=801, Pubmed Id: 15566354, UMLKSK CUI: C0032463
HumanACSL623305acyl-CoA synthetase long-chain family member 6
img GENERIF, Score=734, Pubmed Id: 16572202, UMLKSK CUI: C0032463
HumanMICAL29645microtubule associated monooxygenase, calponin and LIM domain containing 2
img GENERIF, Score=861, Pubmed Id: 16675569, UMLKSK CUI: C0032463
HumanSOCS39021suppressor of cytokine signaling 3
img GENERIF, Score=1000, Pubmed Id: 17325857, UMLKSK CUI: C0032463
HumanSOCS28835suppressor of cytokine signaling 2
img GENERIF, Score=1000, Pubmed Id: 17325857, UMLKSK CUI: C0032463
img NCI, Score=801, Pubmed Id: 17325857, UMLKSK CUI: C0032463
HumanHMGA28091high mobility group AT-hook 2
img NCI, Score=801, Pubmed Id: 17024113, UMLKSK CUI: C0032463
img GENERIF, Score=1000, Pubmed Id: 17854665, UMLKSK CUI: C0032463
HumanTIMP27077TIMP metallopeptidase inhibitor 2
img NCI, Score=801, Pubmed Id: 9359522, UMLKSK CUI: C0032463
img NCI, Score=801, Pubmed Id: 14667201, UMLKSK CUI: C0032463
HumanTIMP17076TIMP metallopeptidase inhibitor 1
img NCI, Score=801, Pubmed Id: 9359522, UMLKSK CUI: C0032463
img NCI, Score=801, Pubmed Id: 14667201, UMLKSK CUI: C0032463
img NCI, Score=801, Pubmed Id: 11920280, UMLKSK CUI: C0032463
HumanTHRA7067thyroid hormone receptor, alpha
img GENERIF, Score=694, Pubmed Id: 17220280, UMLKSK CUI: C0032463
HumanTFRC7037transferrin receptor (p90, CD71)
img NCI, Score=801, Pubmed Id: 9830813, UMLKSK CUI: C0032463
HumanTBXA2R6915thromboxane A2 receptor
img NCI, Score=801, Pubmed Id: 1535462, UMLKSK CUI: C0032463
HumanSTAT5A6776signal transducer and activator of transcription 5A
img GENERIF, Score=734, Pubmed Id: 16684963, UMLKSK CUI: C0032463
img GENERIF, Score=1000, Pubmed Id: 17376889, UMLKSK CUI: C0032463
HumanSTAT36774signal transducer and activator of transcription 3 (acute-phase response factor)
img NCI, Score=801, Pubmed Id: 11378264, UMLKSK CUI: C0032463
HumanPVR5817poliovirus receptor
img GENERIF, Score=660, Pubmed Id: 19011098, UMLKSK CUI: C0032463
HumanPVALB5816parvalbumin
img GENERIF, Score=694, Pubmed Id: 18297277, UMLKSK CUI: C0032463
HumanPROS15627protein S (alpha)
img NCI, Score=801, Pubmed Id: 11104298, UMLKSK CUI: C0032463
img NCI, Score=801, Pubmed Id: 15602345, UMLKSK CUI: C0032463
img NCI, Score=801, Pubmed Id: 8638606, UMLKSK CUI: C0032463
img NCI, Score=801, Pubmed Id: 2148846, UMLKSK CUI: C0032463
img NCI, Score=801, Pubmed Id: 7839322, UMLKSK CUI: C0032463
img NCI, Score=801, Pubmed Id: 11273472, UMLKSK CUI: C0032463
img NCI, Score=801, Pubmed Id: 10782905, UMLKSK CUI: C0032463
HumanPRM25620protamine 2
img GENERIF, Score=734, Pubmed Id: 17113348, UMLKSK CUI: C0032463
HumanTNFRSF11B4982tumor necrosis factor receptor superfamily, member 11b
img GENERIF, Score=1000, Pubmed Id: 15630493, UMLKSK CUI: C0032463
img NCI, Score=801, Pubmed Id: 15630493, UMLKSK CUI: C0032463
HumanNOTCH14851notch 1
img NCI, Score=801, Pubmed Id: 16357566, UMLKSK CUI: C0032463
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0032463Polycythemia Vera0self